Variant #0000551013 (NC_000013.10:g.52585455_52585456del, NM_000053.3:c.19_20del (ATP7B))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52585455_52585456del
DNA change (hg38) g.52011319_52011320del
Published as -
ISCN -
DB-ID ATP7B_000131 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-04 13:54:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP7B NM_000053.3 +/. - c.19_20del r.(?) p.(Gln7AspfsTer14)
ALG11 NM_001004127.2 +/. - c.-1100_-1099del r.(?) p.(=)
UTP14C NM_021645.5 +/. - c.-14105_-14104del r.(?) p.(=)


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